| 영문 | kidney stones | 한글 | 콩팥돌, 콩팥결석 |
|---|---|---|---|
| 설명 | 콩팥의 깔때기 또는 술잔에 형성된 돌을 말하며 요저류, 감염, 요량 감소 등이 있을 때 잘 나타나는 것으로 알려져 있다. 증상은 옆구리나 측복부에 갑자기 생기는 심한 동통, 육안적이나 현미경적 혈뇨, 척추갈비뼈각 압통이 있을 수 있으나 경우에 따라 증상이 없이 우연하게 발견되는 수도 있다. 진단은 요검사나 요배양검사, 혈액검사, 방사선검사를 이용해서 하며 치료방침은 그 돌의 활성도에 따라 다량의 수분 섭취나 진통제를 사용해서 자연배출을 유도하거나 체외충격파 쇄석술, 내비뇨기과적 쇄석술, 수술요법, 내과적 요법을 사용한다. 돌의 활성도란 동통, 폐색현상, 돌의 크기 증가 여부, 새로운 돌의 발생에 의하여 결정되어진다. |
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| 영문 | kidney | 한글 | 콩팥, 신장 |
|---|---|---|---|
| 설명 | 후복벽의 제 11등뼈에서 제 2허리뼈 높이의 복막 바깥에 있는 강낭콩 형태의 장기로서 섬유성 피막과 지방 조직으로 싸여 있다. 무게는 약 130g이며 실질은 겉질과 속질로 나뉘어 진다. |
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| PKD | polycystic kidney disease; proliferative kidney disease |
|---|---|
| ADPKD | autosomal dominant polycystic kidney disease |
| APCD | acquired prothrombin complex deficiency [syndrome]; adult polycystic kidney disease |
| APCKD | adult-type polycystic kidney disease |
| APKD | adult-onset polycystic kidney disease |
| APKD | Adult polycystic kidney disease |
|---|---|
| ADPKD | Autosomal Dominant Polycystic Kidney Disease |
| ARPKD | Autosomal recessive polycystic kidney disease |
| PKD | Polycystic kidney disease |
| PKD1 | Polycystic kidney disease 1 |
| polycystic kidney | A progressive disease characterised by formation of multiple cysts of varying size scattered diffusely throughout both kidney's, resulting in compression and destruction of kidney parenchyma, usually with hypertension, gross haematuria, and uraemia; there are two major types: 1) with onset in infancy or early childhood, usually with autosomal recessive inheritance; 2) with onset in adulthood, with autosomal dominant inheritance. Synonym: polycystic disease of kidneys. (05 Mar 2000) |
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| polycystic kidney disease | <disease> A rare inherited condition in which the kidney are composed of multiple cysts. Kidney cysts are associated with an increased incidence of cerebral aneurysm. Symptoms usually appear later (if they do at all) and include blood in the urine, flank pain, excessive urination at night and abdominal pain. Individuals may also have elevated blood pressure. Chronic (end-stage renal disease) renal failure is the most common result in the 5th to 6th decades of life. Incidence: 1 in 5,000. (02 Jan 1998) |
| disease, polycystic kidney | Genetic (inherited) disorders characterised by the development of innumerable cysts in the kidneys filled with fluid that replace much of the mass of the kidneys and reduce kidney function leading to kidney failure. (12 Dec 1998) |
| kidney, polycystic | Kidney whose tissue is displaced by a large number of tightly packed cysts so that cystic volume predominates over the solid parts to a considerable degree. (12 Dec 1998) |
| kidney, polycystic, autosomal dominant | A genetic disorder with autosomal dominant inheritance characterised by multiple cysts in both kidneys and progressive deterioration of renal function. It is usually caused by a mutant gene at the pkd1 locus on the short arm of chromosome 16, though mutations elsewhere in the genome can also cause the disease. The age of onset of symptoms varies widely. (12 Dec 1998) |
| kidney, polycystic, autosomal recessive | Rare genetic disorder with autosomal recessive inheritance characterised by multiple cysts in both kidneys and associated hepatic lesions. Serious manifestations are usually present at birth and there is high perinatal mortality. (12 Dec 1998) |
| polycystic | Composed of many cysts. (05 Mar 2000) |
| polycystic disease of kidneys | A progressive disease characterised by formation of multiple cysts of varying size scattered diffusely throughout both kidney's, resulting in compression and destruction of kidney parenchyma, usually with hypertension, gross haematuria, and uraemia; there are two major types: 1) with onset in infancy or early childhood, usually with autosomal recessive inheritance; 2) with onset in adulthood, with autosomal dominant inheritance. Synonym: polycystic disease of kidneys. (05 Mar 2000) |
| polycystic liver | Gradual cystic dilation of intralobular bile ducts (Meyenburg's complexes) that fail to involute in embryologic development of the liver; frequently associated with bilateral congenital polycystic kidneys and occasionally with cystic involvement of the pancreas, lungs, and other organs. Synonym: polycystic liver disease. (05 Mar 2000) |
| polycystic liver disease | Gradual cystic dilation of intralobular bile ducts (Meyenburg's complexes) that fail to involute in embryologic development of the liver; frequently associated with bilateral congenital polycystic kidneys and occasionally with cystic involvement of the pancreas, lungs, and other organs. Synonym: polycystic liver disease. (05 Mar 2000) |
| polycystic ovarian disease | <disease> A condition found among women who do not ovulate, characterised by multiple ovarian cysts and increased androgen production. (09 Oct 1997) |
| polycystic ovary | Enlarged cystic ovary's, pearl white in colour, with thickened tunica albuginea, characteristic of the Stein-Leventhal syndrome; clinical features are abnormal menses, obesity, and evidence of masculinization, such as hirsutism. (05 Mar 2000) |
| polycystic ovary syndrome | <syndrome> Clinical symptom complex characterised by oligomenorrhoea or amenorrhoea, anovulation, and regularly associated with bilateral polycystic ovaries. (12 Dec 1998) |
| disease, ovarian, polycystic | See Disease, polycystic ovarian. (12 Dec 1998) |
| disease, polycystic ovarian | An hormonal problem that causes women to have a variety of symptoms including irregular or no periods, acne, obesity and excessive hair growth. Women with PCO are at a higher risk for uterine cancer (endometrial cancer), diabetes, high blood pressure, and heart disease. With proper treatment, risks can be minimised. PCO is also known as Stein-Leventhal syndrome. (12 Dec 1998) |
| polycystic kidney d. |
either of two unrelated heritable disorders marked by cysts scattered throughout both kidneys. Autosomal dominant polycystic kidney disease (ADPKD, formerly called the adult form) is the most common renal cystic condition, with deterioration of renal function that may not be detectable until the third or fourth decade of life; it runs a variable course, with only some cases progressing to renal failure. Autosomal recessive polycystic kidney disease (ARPKD, formerly called the infantile form) may be congenital or may appear at any time during childhood and has a high perinatal mortality rate, with almost all cases leading to hypertension; in older children it may be associated with cystic and fibrotic disease of the liver. A similar acquired disease sometimes accompanies end-stage renal disease and is called acquired cystic disease of kidney. Called also polycystic kidneys and polycystic renal d.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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